Mangesi Lindeka, Hofmeyr G Justus, Smith Valerie, Smyth Rebecca M D
Epidemiological Research and Surveillance Management Directorate, Eastern Cape Department of Health, Private Bag X0038, Bisho, South Africa, 5605.
Cochrane Database Syst Rev. 2015 Oct 15;2015(10):CD004909. doi: 10.1002/14651858.CD004909.pub3.
Fetal movement counting is a method by which a woman quantifies the movements she feels to assess the condition of her baby. The purpose is to try to reduce perinatal mortality by alerting caregivers when the baby might be compromised. This method may be used routinely, or only in women who are considered at increased risk of complications affecting the baby. Fetal movement counting may allow the clinician to make appropriate interventions in good time to improve outcomes. On the other hand, fetal movement counting may cause unnecessary anxiety to pregnant women, or elicit unnecessary interventions.
To assess outcomes of pregnancy where fetal movement counting was done routinely, selectively or was not done at all; and to compare different methods of fetal movement counting.
We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (31 May 2015) and reference lists of retrieved studies.
Randomised controlled trials (RCTs) and cluster-RCTs where fetal movement counting was assessed as a method of monitoring fetal wellbeing.
Two review authors assessed studies for eligibility, assessed the methodological quality of included studies and independently extracted data from studies. Where possible the effects of interventions were compared using risk ratios (RR), and presented with 95% confidence intervals (CI). For some outcomes, the quality of the evidence was assessed using the GRADE approach.
Five studies (71,458 women) were included in this review; 68,654 in one cluster-RCT. None of these five trials were assessed as having low risk of bias on all seven risk of bias criteria. All included studies except for one (which included high-risk women as participants) included women with uncomplicated pregnancies.Two studies compared fetal movement counting with standard care, as defined by trial authors. Two included studies compared two types of fetal movement counting; once a day fetal movement counting (Cardiff count-to-10) with more than once a day fetal movement counting methods. One study compared fetal movement counting with hormone assessment.(1) Routine fetal movement counting versus mixed or undefined fetal movement countingNo study reported on the primary outcome 'perinatal death or severe morbidity'. In one large cluster-RCT, there was no difference in mean stillbirth rates per cluster (standard mean difference (SMD) 0.23, 95% CI -0.61 to 1.07; participants = 52 clusters; studies = one, low quality evidence). The other study reported no fetal deaths. There was no difference in caesarean section rate between groups (RR 0.93, 95% CI 0.60 to 1.44; participants = 1076; studies = one,low quality evidence). Maternal anxiety was significantly reduced with routine fetal movement counting (SMD -0.22, 95% CI -0.35 to -0.10; participants = 1013; studies = one, moderate quality evidence). Maternal-fetal attachment was not significantly different (SMD -0.02, 95% CI -0.15 to 0.11; participants = 951; studies = one, low quality evidence). In one study antenatal admission after reporting of decreased fetal movements was increased (RR 2.72, 95% CI 1.34 to 5.52; participants = 123; studies = one). In another there was a trend to more antenatal admissions per cluster in the counting group than in the control group (SMD 0.38, 95% CI -0.17 to 0.93; participants = 52 clusters; studies = one, low quality evidence). Birthweight less than 10th centile was not significantly different between groups (RR 0.98, 95% CI 0.66 to 1.44; participants = 1073; studies = one, low quality evidence). The evidence was of low quality due to imprecise results and because of concerns regarding unclear risk of bias. (2) Formal fetal movement counting (Modified Cardiff method) versus hormone analysisThere was no difference between the groups in the incidence of caesarean section (RR 1.18, 95% CI 0.83 to 1.69; participants = 1191; studies = one). Women in the formal fetal movement counting group had significantly fewer hospital visits than those randomised to hormone analysis (RR 0.26, 95% CI 0.20 to 0.35), whereas there were fewer Apgar scores less than seven at five minutes for women randomised to hormone analysis (RR 1.72, 95% CI 1.01 to 2.93). No other outcomes reported showed statistically significant differences. 'Perinatal death or severe morbidity' was not reported. (3) Formal fetal movement counting once a day (count-to-10) versus formal fetal movement counting method where counting was done more than once a day (after meals)The incidence of caesarean section did not differ between the groups under this comparison (RR 2.33, 95% CI 0.61 to 8.99; participants = 1400; studies = one). Perinatal death or severe morbidity was not reported. Women were more compliant in using the count-to-10 method than they were with other fetal movement counting methods, citing less interruption with daily activities as one of the reasons (non-compliance RR 0.25, 95% CI 0.19 to 0.32).Except for one cluster-RCT, included studies were small and used different comparisons, making it difficult to measure the outcomes using meta-analyses. The nature of the intervention measured also did not allow blinding of participants and clinicians..
AUTHORS' CONCLUSIONS: This review does not provide sufficient evidence to influence practice. In particular, no trials compared fetal movement counting with no fetal movement counting. Only two studies compared routine fetal movements with standard antenatal care, as defined by trial authors. Indirect evidence from a large cluster-RCT suggested that more babies at risk of death were identified in the routine fetal monitoring group, but this did not translate to reduced perinatal mortality. Robust research by means of studies comparing particularly routine fetal movement counting with selective fetal movement counting is needed urgently, as it is a common practice to introduce fetal movement counting only when there is already suspected fetal compromise.
胎动计数是一种让孕妇量化自身所感觉到的胎动,以评估胎儿状况的方法。其目的是在胎儿可能受到损害时向护理人员发出警报,从而试图降低围产期死亡率。这种方法可以常规使用,也可仅用于那些被认为胎儿出现并发症风险增加的孕妇。胎动计数或许能让临床医生及时进行适当干预,以改善结局。另一方面,胎动计数可能会给孕妇带来不必要的焦虑,或引发不必要的干预措施。
评估常规进行、选择性进行或根本不进行胎动计数的妊娠结局;并比较不同的胎动计数方法。
我们检索了Cochrane妊娠与分娩组试验注册库(2015年5月31日)以及检索到的研究的参考文献列表。
将胎动计数作为监测胎儿健康状况方法进行评估的随机对照试验(RCT)和整群随机对照试验(cluster-RCT)。
两位综述作者评估研究是否符合纳入标准,评估纳入研究的方法学质量,并独立从研究中提取数据。若有可能,使用风险比(RR)比较干预措施的效果,并给出95%置信区间(CI)。对于某些结局,使用GRADE方法评估证据质量。
本综述纳入了5项研究(71458名女性);其中一项整群随机对照试验纳入了68654名女性。这5项试验中没有一项在所有7条偏倚风险标准上被评估为低偏倚风险。除一项研究(其纳入高危女性作为参与者)外,所有纳入研究均包括无并发症妊娠的女性。两项研究将胎动计数与试验作者所定义的标准护理进行了比较。两项纳入研究比较了两种胎动计数类型;每日一次胎动计数(加的夫10次计数法)与每日多次胎动计数方法。一项研究将胎动计数与激素评估进行了比较。(1)常规胎动计数与混合或未明确的胎动计数在主要结局“围产期死亡或严重发病”方面,没有研究进行报告。在一项大型整群随机对照试验中,每群的平均死产率没有差异(标准化均数差(SMD)0.23,95%CI -0.61至1.07;参与者 = 52群;研究 = 1项,低质量证据)。另一项研究未报告胎儿死亡情况。两组间剖宫产率没有差异(RR 0.93,95%CI 0.60至1.44;参与者 = 1076;研究 = 1项,低质量证据)。常规胎动计数可显著降低产妇焦虑(SMD -0.22,95%CI -0.35至 -0.10;参与者 = 1013;研究 = 1项,中等质量证据)。母婴依恋没有显著差异(SMD -0.02,95%CI -0.15至0.11;参与者 = 951;研究 = 1项,低质量证据)。在一项研究中,报告胎动减少后产前入院人数增加(RR 2.72,95%CI 1.34至5.52;参与者 = 123;研究 = 1项)。在另一项研究中,计数组每群的产前入院人数有多于对照组的趋势(SMD 0.38,95%CI -0.17至0.93;参与者 = 52群;研究 = 1项,低质量证据)。两组间出生体重低于第10百分位数的情况没有显著差异(RR 0.98,95%CI 0.66至1.44;参与者 = 1073;研究 = 1项,低质量证据)。由于结果不精确以及对偏倚风险不明确的担忧,证据质量较低。(2)正式胎动计数(改良加的夫方法)与激素分析两组间剖宫产发生率没有差异(RR 1.18,95%CI 0.83至1.69;参与者 = 1191;研究 = 1项)。正式胎动计数组的女性医院就诊次数显著少于随机分配至激素分析组的女性(RR 0.26,95%CI 0.20至0.35),而随机分配至激素分析组的女性5分钟时Apgar评分低于7分的情况较少(RR 1.72,95%CI 1.01至2.93)。报告的其他结局均未显示出统计学显著差异。未报告“围产期死亡或严重发病”情况。(3)每日一次正式胎动计数(10次计数法)与每日多次正式胎动计数方法(饭后)在此比较中,两组间剖宫产发生率没有差异(RR 2.33,95%CI 0.61至8.99;参与者 = 1400;研究 = 1项)。未报告围产期死亡或严重发病情况。女性使用10次计数法比使用其他胎动计数方法的依从性更高,她们将对日常活动干扰较少作为原因之一(不依从RR 0.25,95%CI 0.19至0.32)。除一项整群随机对照试验外,纳入研究规模较小且采用了不同的比较方法,使得难以使用Meta分析来衡量结局。所测量的干预措施性质也不允许对参与者和临床医生进行盲法处理。
本综述未提供足够证据来影响实践。特别是,没有试验将胎动计数与不进行胎动计数进行比较。只有两项研究将常规胎动与试验作者所定义的标准产前护理进行了比较。一项大型整群随机对照试验的间接证据表明,在常规胎儿监测组中识别出了更多有死亡风险的婴儿,但这并未转化为围产期死亡率的降低。迫切需要通过特别比较常规胎动计数与选择性胎动计数的研究进行有力研究,因为仅在已经怀疑胎儿受到损害时才引入胎动计数是一种常见做法。